Evidence map›Paper›PMID 37957582›Full record

ArticleBMC bioinformatics2023

A novel two-way rebalancing strategy for identifying carbonylation sites.

Linjun Chen, Xiao-Yuan Jing, Yaru Hao, Wei Liu, Xiaoke Zhu, Wei Han

Abstract read
In one paragraph

Article in BMC bioinformatics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Explainable Deep Multilevel Attention Learning for Predicting Protein Carbonylation Sites.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Linjun ChenSchool of Computer Science, Wuhan University, Wuhan, China.
Xiao-Yuan JingSchool of Computer Science, Wuhan University, Wuhan, China. jingxy_2000@126.com.
Yaru HaoSchool of Computer Science, Wuhan University, Wuhan, China.
Wei LiuSchool of Computer Science, Wuhan University, Wuhan, China.
Xiaoke ZhuSchool of Computer and Information Engineering, Henan University, Kaifeng, China.
Wei HanSchool of Computer Science, Wuhan University, Wuhan, China.

Funding

Innovation Group of Guangdong Education Department under Grant No.2020KCXTD014Key Scientific and Technological Project of Henan Province of China No. 232102211013NSFC Project under Grant Nos.62176069 and 61933013
6 · The paper itself

Abstract

backgroundAs an irreversible post-translational modification, protein carbonylation is closely related to many diseases and aging. Protein carbonylation prediction for related patients is significant, which can help clinicians make appropriate therapeutic schemes. Because carbonylation sites can be used to indicate change or loss of protein function, integrating these protein carbonylation site data has been a promising method in prediction. Based on these protein carbonylation site data, some protein carbonylation prediction methods have been proposed. However, most data is highly class imbalanced, and the number of un-carbonylation sites greatly exceeds that of carbonylation sites. Unfortunately, existing methods have not addressed this issue adequately.

resultsIn this work, we propose a novel two-way rebalancing strategy based on the attention technique and generative adversarial network (Carsite_AGan) for identifying protein carbonylation sites. Specifically, Carsite_AGan proposes a novel undersampling method based on attention technology that allows sites with high importance value to be selected from un-carbonylation sites. The attention technique can obtain the value of each sample's importance. In the meanwhile, Carsite_AGan designs a generative adversarial network-based oversampling method to generate high-feasibility carbonylation sites. The generative adversarial network can generate high-feasibility samples through its generator and discriminator. Finally, we use a classifier like a nonlinear support vector machine to identify protein carbonylation sites.

conclusionsExperimental results demonstrate that our approach significantly outperforms other resampling methods. Using our approach to resampling carbonylation data can significantly improve the effect of identifying protein carbonylation sites.

Indexed as

Protein Processing, Post-TranslationalProteinsHumansProtein CarbonylationSupport Vector MachineProteinsAttention techniqueGenerative adversarial networksIdentifying protein carbonylation sitesProtein carbonylationRebalance

Identifiers

PMID37957582
PMCPMC10644465

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.